rs145394391

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs145394391(C;T)

Make rs145394391(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

95171078

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs145394391
dbSNP (classic)	rs145394391
ClinGen	rs145394391
ebi	rs145394391
HLI	rs145394391
Exac	rs145394391
Gnomad	rs145394391
Varsome	rs145394391
LitVar	rs145394391
Map	rs145394391
PheGenI	rs145394391
Biobank	rs145394391
1000 genomes	rs145394391
hgdp	rs145394391
ensembl	rs145394391
geneview	rs145394391
scholar	rs145394391
google	rs145394391
pharmgkb	rs145394391
gwascentral	rs145394391
openSNP	rs145394391
23andMe	rs145394391
SNPshot	rs145394391
SNPdbe	rs145394391
MSV3d	rs145394391
GWAS Ctlg	rs145394391

Max Magnitude

0

ClinVar
Risk	rs145394391(T;T)
Alt	rs145394391(T;T)
Reference	Rs145394391(C;C)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia
Reversed	0
HGVS	NC_000009.11:g.97933360C>T
CLNSRC
CLNACC	RCV000230742.1,